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Oncogenesis|October 13, 2021
Inactivation of the CIC-DUX4 oncogene through P300/CBP inhibition, a therapeutic approach for CIC-DUX4 sarcomaDarko Bosnakovski, Elizabeth T Ener, Mark S Cooper, et al.RSC Chemical Biology|October 6, 2023
Chirality: a key parameter in chemical probesAndrew McGown, Jordan Nafie, Mohammed Otayfah, et al.Journal of Medicinal Chemistry|January 16, 2025
Structure-Based Optimization of Pyridone α-Ketoamides as Inhibitors of the SARS-CoV-2 Main ProteaseRavi Kumar Akula, Haifa El Kilani, Alina Metzen, et al.RSC Medicinal Chemistry|March 17, 2025
Development of p300-targeting degraders with enhanced selectivity and onset of degradationGraham P Marsh, Mark S Cooper, Sean Goggins, et al.Journal of Medicinal Chemistry|September 30, 2022
Diastereomeric Resolution Yields Highly Potent Inhibitor of SARS-CoV-2 Main ProteaseMark S Cooper, Linlin Zhang, Mohamed Ibrahim, et al.Organic & Biomolecular Chemistry|October 6, 2023
Efficient, multi-hundred-gram scale access to E3 ubiquitin ligase ligands for degrader developmentMark S Cooper, Mark C Norley, Simon Armitage, et al.Nature Communications|May 13, 2026
BromoCatch: a self-labelling tag platform for protein modification and live cell imagingMaria Rodriguez-Rios, Conner Craigon, Mark A Nakasone, et al.Journal of Medicinal Chemistry|April 17, 2025
Structure-Guided Design of ISOX-DUAL-Based Degraders Targeting BRD4 and CBP/EP300: A Case of Degrader CollapseAnthony K Edmonds, Dimitrios-Ilias Balourdas, Graham P Marsh, et al.Pageof 2